Michael L. Netzloff

High-resolution array CGH defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with microdeletions of 1q43q44

Blake C. Ballif, Jill A. Rosenfeld, Ryan N. Traylor et al. · Human Genetics · 2011 · 147 citations

Life Sciences, Genetics, Neuroscience +17

Abnormal sterol metabolism in a patient with Antley‐Bixler syndrome and ambiguous genitalia

Richard I. Kelley, Lisa E. Kratz, Rivka L. Glaser et al. · American Journal of Medical Genetics · 2002 · 97 citations

Life Sciences, Genetics, Molecular Genetics +17

The role of inhibited cell-cell communication in teratogenesis

James E. Trosko, Chia‐Cheng Chang, Michael L. Netzloff · Teratogenesis Carcinogenesis and Mutagenesis · 1982 · 76 citations

Medicine, Cell Biology, Developmental Biology +13

Sensorineural hearing loss in children and adults with Williams syndrome

Jeffrey A. Marler, Jill L. Elfenbein, Brenda M. Ryals et al. · American Journal of Medical Genetics Part A · 2005 · 67 citations

Health Professions, Audiology, Pediatrics +17

Identification of constitutively activating mutation of the luteinising hormone receptor in a family with male limited gonadotrophin independent precocious puberty (testotoxicosis).

N. Kawate, Gad B. Kletter, B E Wilson et al. · Journal of Medical Genetics · 1995 · 51 citations · Full text

Medicine, Endocrinology, Genetics +12